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Program Evaluation Coordinator
4 months ago
Duties
: Collaborates within the team through active engagement in exchange of research ideas and findings pertinent to Prompt clinic client service Draft/review research related documentation, consent forms and data collection/interview instruments Lead in the development of program evaluation, outcome and follow-up Liaise with research collaborators, research team members, Research Ethics Board Complete regulatory documentation as required, including research ethics Facilitate the planning and coordination of research study protocol(s), and the establishment of policies and procedures Guarantee capture and cleaning of data (wait times, waitlist, etc) Collaborate on development and implementation of user-friendly summary data reports for program evaluation, clinical, and research purposes Ability to perform statistical analyses including power analyses, univariate, multivariate and non-parametric statistics using SPSS-PC Assist with literature searches of various literature databases and use appropriate search criteria Develop and maintain a comprehensive clinical research database Management of non-health records files Coordinate the administration of standardized intake and pre/post measures Sort, monitor and maintain measurement and outcomes based care database Maintain a database of bibliographic references Coordinate, edit and assist in drafting grant applications, abstracts, manuscripts, journal articles, letters to the editor, reports and research protocols Report generation and communication distribution Recruit, instruct and coordinate research participants appropriately Work in a manner that is in compliance with staff and patient/client safety practices, policies and procedures of The Royal. Ensure a work environment that is conducive to The Royals Anti-Racism, Harassment and Discrimination Free Workplace Policy. Qualifications: Masters degree in Health, Science, Medical or other relevant discipline with 2+ years of experience in a clinical/medical research environment OR Bachelors degree in relevant discipline with 2+ years of experience in clinical/medical research environment Specific clinical education, certification and/or licensure requirements may exist for individual positions in this classification Ability to communicate and interact competently and professionally at all levels within varied environments Skill in collecting, validating, analyzing and manipulating research data Advanced knowledge of computer programs, including research related and statistical analysis software Knowledge of research principles, methodology and procedures Ability to work on several projects concurrently Ability to develop and implement clinical research plans and standard operating procedures Ability to design and implement systems necessary to collect, maintain and analyze data Self-directed and able to work independently and within an interdisciplinary team Detail oriented and highly organized Excellent interpersonal skills Previous experience in clinical research including subject recruitment is an asset Ability to communicate and interact competently and professionally at all levels within a broad, complex clinical research environment. Good working knowledge of ICH Good Clinical Practices and relevant regulations, legislation and guidelines applicable to the clinical research field Knowledge of medical and research terminology Advanced proficiency with Microsoft Excel Ability to follow data collection and management guidelines Perform other job duties as assigned English level A- is mandatory in oral expression, oral comprehension, reading comprehension and written expression. Bilingual (French/English) is considered an asset. Salary Range: $39.16 to $50.77 (BA) to $44.67 to 57.90 (MA) per hour